A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6581650



Internal ID20954721
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:102944654..102945241hg38UCSC Ensembl
chr11:102815383..102815970hg19UCSC Ensembl
Cytoband11q22.2
Allele length
AssemblyAllele length
hg38588
hg19588
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18234343
Samples
Known GenesMMP13
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6581650
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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